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Combined α-thalassemia and Hemoglobin J-Iran (β77 His → Asp). A Family Study in southern Iran
Hb J-Iran α-thalassemia Hemoglobin variants Electrophoresis High performance liquid chromatography
2015/9/23
We report a 23-year-old man and three members of his family with Hb J-Iran confirmed by electrophoresis, chain separation by high performance liquid chromatography and sequencing. Alpha thalassemia wa...
Hemoglobin D (Hb D Punjab/ Los Angeles and Hb D Iran) and Co-Inheritance with Alpha- and Beta-Thalassemia in southern Iran
Hemoglobin (Hb) D Punjab Hb D Iran Hb D- beta- thalassemia (thal) Hb D-alpha- thal-1 trait Hb DSickle cell anemia
2015/9/23
Background: Hemoglobin-D (Hb D) is an uncommon structural hemoglobin variant, which is reported to be prevalent in north western India. There are only a few small series, of this entity in the literat...
Sickle cell hemoglobin D disease First reported case in IRAN
Sickle cell hemoglobin D IRAN
2009/12/15
A case of sickle cell Hb D disease IS reported in young Iranian male.the father of whom carried an AS sickle cell trait and the mother an AD trait.This disease was diagnosed by Hb electrophoresis.aga...
The comparison of Hemoglobin and Mean Corpuscular Volume in gestational diabetes mellitus women and healthy women
Hemoglobin Mean Corpuscular Volume Gestational Diabetes Mellitus
2009/12/2
Background & Aim: Screening methods of gestational diabetes mellitus (GDM) diagnosis is controversy. The survey of relation between GDM and its risk factors helps to determine screening methods. This ...
